Lung Cancer Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
- People who are willing to take part and have signed a consent form agreeing to join the study
- People aged 18 to 74 years old (any gender)
- People whose general physical health is rated as fully active or able to carry out light work, based on a standard medical scoring system called ECOG (scores 0 or 1)
- People whose doctors expect them to live for at least 12 months
- People who have been confirmed by tissue testing to have a type of lung cancer called non-small cell lung cancer (NSCLC) that is located in the outer part of the lung, at a stage between IIA and IIIB (using IASLC 9th edition staging), and whose cancer does not have certain genetic changes known as EGFR mutations or ALK rearrangements
- People whose cancer is contained within a single section (lobe) of the lung, with no solid tumours spread across different lobes
- People who have not had open chest surgery on the same side of the chest before
- People who have already completed 2 to 4 cycles of pre-surgery treatment (called neoadjuvant therapy) involving both an immunotherapy drug (a PD-1 or PD-L1 inhibitor) and a two-drug platinum-based chemotherapy combination
- People whose heart and lung function is considered sufficient for surgery, including specific breathing test results (FEV1 of at least 1.5 L or a lung gas exchange measure called DLCO of at least 40%), as assessed by the treating doctor
- People whose tumour is more than 2 cm away from the airway opening, based on a pre-surgery CT scan
- People whose tumour has been assessed by a review committee as suitable for a specific type of lung surgery that removes less than a full lobe, while completely removing the cancer (called sub-lobe R0 resection)
Who may not be able to join:
- People who are not expected to tolerate a full lobe removal surgery (lobectomy)
- People who have received radiation therapy to the chest before the planned surgery
- People who have had a transplant of donated tissue or a solid organ (such as a kidney or liver)
- People who have been diagnosed with an autoimmune disease, or who have been taking steroid medication (such as prednisone at more than 10 mg per day) or other immune-suppressing treatments within the 3 months before surgery
- People who have a history of a non-infectious lung scarring condition (interstitial lung disease) that has required steroid treatment, or who currently have this condition and need steroid treatment for it
- People who test positive for HIV, or who have active hepatitis B or active hepatitis C, based on blood tests done during the screening period
- People with high blood pressure that is not well controlled by medication, meaning blood pressure readings remain above 150/90 mmHg on average across the three most recent measurements taken before joining the study
- People who have an active infection during the screening period that still requires intravenous (drip) antibiotic or antiviral treatment
- People who have had another cancer (other than certain low-risk or fully treated cancers such as skin basal cell cancer, cervical or breast cancer in situ, superficial bladder cancer, or localised prostate cancer) within the 3 years before signing the consent form — though people with low-risk early prostate cancer under stable active monitoring or who have received curative treatment may still be considered eligible (confirm with trial site)
- People whose situation, in the treating doctor's judgement, could interfere with the study results or for whom participation would not be in their best interest
- People who are pregnant, breastfeeding, or planning to become pregnant, or who have a positive pregnancy blood test within 7 days before starting the study treatment
- People who are unlikely to follow the study procedures or are unwilling or unable to complete the full study process
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Phone: +8616620072467
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
3y-DFS
Can't join this trial?
Data last synced from ClinicalTrials.gov: 28 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.